Protocol for the specified clinical experience investigation on the single use of Casodex® Tablet 80 mg - CAMON
Study identifier:NIS-OJP-CAS-2009/1
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Study Complete
Official Title
Protocol for the specified clinical experience investigation on the single use of Casodex® Tablet 80 mg
Medical condition
prostate cancer
Phase
-
Healthy volunteers
No
Study drug
-
Sex
Male
Actual Enrollment
712
Study type
Observational
Age
N/A
Date
Study Start Date: 01 May 2009
Primary Completion Date: 01 Mar 2012
Study Completion Date: 01 Mar 2012
Study design
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verification:
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
Sponsors
AstraZeneca Pharmaceuticals
Collaborators
-
Inclusion and exclusion criteria
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